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Urine cattle

Urine (cattle) Extraction, fractionation by cation and anion exchange chromatography, p-glucuronidase/sulphatase hydrolysis HPLC/lon Trap-MS HPLC/MS No data 76.2 2.3% Coldham et al. 1998... [Pg.139]

About 50% of copper in food is absorbed, usually under equitibrium conditions, and stored in the tiver and muscles. Excretion is mainly via the bile, and only a few percent of the absorbed amount is found in urine. The excretion of copper from the human body is influenced by molybdenum. A low molybdenum concentration in the diet causes a low excretion of copper, and a high intake results in a considerable increase in copper excretion (68). This copper—molybdenum relationship appears to correlate with copper deficiency symptoms in cattle. It has been suggested that, at the pH of the intestine, copper and molybdate ions react to form biologically unavailable copper molybdate (69). [Pg.212]

At low doses, the metabolism of diisopropyl methylphosphonate to IMPA in the body is rapid and nearly complete. After oral exposure to diisopropyl methylphosphonate, the principal metabolite isolated from both urine (93-99%) and feces ( 97%) in mink, mice, rats, dogs, and cattle is IMPA (Bucci et al. 1992 Hart 1976 Ivie 1980). Less than 0.5% of the radiolabel was detected in the exhaled air of rats and mice as carbon dioxide after diisopropyl methylphosphonate ingestion (Hart 1976). Thus, complete metabolism of diisopropyl methylphosphonate occurs only to a minor extent. [Pg.70]

After exerting their action in the organism, natural and synthetic hormones are catabolized in the liver by conjugation to glucuronide and/or sulfate moieties, forming more polar conjugated forms which are excreted via urine. This is the main route of hormone excretion in humans and pigs. A fraction of hormones is also excreted in a free form via feces in animals such as sheep and cattle this is the main route for hormone excretion (Table 3) [66, 67],... [Pg.83]

Oral treatment of sheep and cattle (Bos spp.) with diflubenzuron is followed by absorption of the compound through the gastrointestinal tract, metabolism, and elimination of residues through the urine, feces, and, to a very limited extent, milk. Intact diflubenzuron is eliminated in the feces of orally dosed cattle and sheep (Ivie 1978). Major metabolites of diflubenzuron excreted by cattle and sheep result from hydroxylation on the difluorobenzoyl and chlorophenyl rings, and by cleavage between the carbonyl and amide groups to produce metabolites that are excreted free or as conjugates (Ivie 1978). Cattle dosed repeatedly with diflubenzuron had detectable residues only in liver... [Pg.1011]

Urinary proteins were analyzed by SDS-polyacrylamide gel electrophoresis (PAGE), and a 70-kDa protein was identified as the major component of cat urine (Fig. 4.1 A). Comparative analysis of urinary proteins in several other mammals such as humans, mice, dogs, and cattle did not detect a 70-kDa protein. Therefore, the 70-kDa protein was purified from cat urine and characterized by biochemical methods (Miyazaki, Kamiie, Soeta, Taira and Yamashita 2003). Analysis of tissue distribution indicated that the 70-kDa protein is expressed in the kidney in a tissue-specific manner and secreted from the proximal straight tubular cells of the kidney into the urine (Fig. 4.IB). A full-length cDNA for a 70-kDa protein was cloned from a cat kidney cDNA library. The cDNA clone encoded a polypeptide of 545 amino acid residues. The deduced amino acid sequence shared 47% identity with cat carboxylesterase (CES, EC 3.1.1.1), and contained both the CES family protein motif (EDCLY) and a conserved active site motif (GESAG) associated with... [Pg.52]

For obvious practical and commercial reasons, the sex attractant(s) of livestock have received considerable attention. In cattle, experiments have shown that bulls responses to sex odors depend on the breeding regimen. Free-ranging bulls with access to cows will prefer to mount a cow that had been scented with urine from an estrous cow to one carrying the urine odor of an anestrous cow. Bulls kept tied up indoors and encountering cows in stalls mount cows indiscriminately (Sambraus and Waring, 1975). [Pg.185]

Bursell, E., Gough, A. J. E., Beevor, P. S., etal. (1988). Identification of components of cattle urine attractive to tsetse flies, Glossina spp. (Diptera Glossinidae). Bulletin of Entomological Research 78,281-291. [Pg.442]

Weeth, H.J., C.F. Speth, and D.R. Hanks. 1981. Boron content of plasma and urine as indicators of boron intake in cattle. Amer. Jour. Vet. Res. 42 474-477. [Pg.1589]

The absorption of spectinomycin is poor via the oral route, but rapid and extensive after intramuscular injection. It is not extensively metabolized in animals and rapidly excreted in the urine (16). Following subcutaneous injections of spectinomycin sulfate to cattle, 70-83% of the dose was excreted in the urine and 62-64% of this was parent spectinomycin (17). Several minor metabolites were found in the urine that consisted mostly of dihydroxyspectinomycin and two acetylated isomers, and an unusual ammoniated spectinomycin metabolite and its acetylated derivative. There was also some evidence, but it was not compelling, for a spectinomycin sulfate conjugate. Dihydrospectinomycin and parent spectinomycin were the only identifiable major components found in the liver and the kidney, respectively. Liver and kidney retained the highest concentrations of total residues throughout the 15-day withdrawal period. [Pg.36]

Results of pharmacokinetic studies of streptomycin are in most cases also applicable to dihydrostreptomycin and vice versa. In animals, the absorption of both streptomycin and dihydrostreptomycin is poor via the oral route but rapid after intramuscular administration. In cattle, peak serum levels were obtained 1 h after intramuscular injection of either streptomycin or dihydrostreptomycin (18), whereas serum concentrations produced in sheep and horses paralleled those obtained in cattle (19). As a result, most of an oral dose is recovered in the feces whereas most of a parenteral dose is recovered in the urine. However, if kidney function is severely impaired, little of an intramuscularly administered dose is excreted in the urine. [Pg.37]

Cephalexin is quickly absorbed and metabolized to unidentified compounds in cattle, sheep, and swine. It is principally excreted in urine but small amounts are also excreted by liver in bile. No detectable residues (limit of detection 60 ppb) were found in cows, in sheep and swine slaughtered at 4 and 10 days, respectively, after receiving intramuscularly 7 mg cephalexin sodiurn/kg bw/day for 5 consecutive days. No detectable residues were found in sheep and swine slaughtered 3 and 2 days, respectively, after receiving 10 mg cephalexin sodium/ kg bw/day intramuscularly for 5 consecutive days. [Pg.54]

Ceftiofiir is absorbed poorly after oral administration but rapidly after intramuscular injection. In all species, ceftiofur was rapidly metabolized to desfuroyl-ceftioftir and fiiroic acid. Desfiiroylceftiofur occurred in the free form in the plasma of treated cattle but was covalently bound to plasma proteins in rats (82). Maximum blood concentrations of ceftiofiir-related residues were achieved within 0.5 and 2 h of dosing. Unmetabolized ceftiofur was generally undetectable in blood within 2-4 h of dosing (83). More than 90% of the administered dose was excreted within 24 h of administration, mostly in urine. Residues in urine and feces were composed primarily of desfiiroylceftiofur and desfiiroylceftiofur cysteine disulfide, with small amounts of unmetabolized ceftiofur. [Pg.57]

After intramuscular injections of radiolabeled ceftiofur to cattle and swine, the compound was absorbed rapidly into the blood and eliminated mostly in urine (84). The tissue in which highest residue concentrations were observed at 12 h after the last dose was the kidney. Most of the radioactivity was found in the form of the microbiologically active primary metabolite, desfiiroylceftiofur, conjugated to macromolecules in plasma and tissues. Desfiiroylceftiofur cysteine was also found in tissues, plasma, and urine, whereas the desfiiroylceftiofur dimer was found in urine. It was suggested that since the binding of desfiiroylceftiofur to biological molecules is reversible, all of the ceftiofiir-related residues that contain the desfuroylceftiofur moiety have the potential to be microbiologically active. [Pg.57]

The extent to which a sulfonamide is acetylated depends upon the drug administered and the animal species. Acetylsulfathiazole is the principal metabolite found in the urine of cattle, sheep, and swine after enteral or parenteral administration of sulfathiazole. However, sheep can acetylate only 10% of the dose, while cattle can acetylate 32%, and swine 39%. When sulfamethazine was administered intravenously or orally to cattle, the animals eliminated 11% or 25% of the dose, respectively, in urine as N" -acetylsulfamethazine. The increased acetylation that occurred following tlie oral administration may be related to the increased exposure of sulfamethazine to liver enzymes following its absorption into the portal circulation. The acetylation rate may also be affected by the health status of an animal. Tims, cows suffering from ketosis in cows acetylate sulfonamides at much lower extent. [Pg.88]

Baquiloprim has a high oral bioavailability in animals where it is widely distributed in the body and slowly eliminated (222,223). In cattle, baquiloprim was reported to have a much longer half-life and a larger volume of distribution than trimethoprim (223). Both urine and bile are important routes of elimination. [Pg.93]

Upon intramammary administration to cattle, novobiocin is rapidly absorbed and excreted through milk, feces, and urine. Detectable residues are present in milk for a few days after intramammary infusion, the elimination being highly depended on dosage and formulation. One day after treatment, the concentrations of microbiologically active residues in the liver, kidney, and udder tissue were in the range 1-4 ppm, whereas concentrations in muscle and fat were below 0.1 ppm. [Pg.100]


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See also in sourсe #XX -- [ Pg.27 , Pg.28 , Pg.29 , Pg.30 , Pg.31 , Pg.32 , Pg.33 ]




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